Immunotherapy of experimental melanoma with ICOS-Fc loaded in biocompatible and biodegradable nanoparticles.
Controlled release
ICOS-L
Melanoma
PLGA nanoparticles
β-Cyclodextrin nanosponges
Journal
Journal of controlled release : official journal of the Controlled Release Society
ISSN: 1873-4995
Titre abrégé: J Control Release
Pays: Netherlands
ID NLM: 8607908
Informations de publication
Date de publication:
10 04 2020
10 04 2020
Historique:
received:
09
09
2019
revised:
15
01
2020
accepted:
17
01
2020
pubmed:
22
1
2020
medline:
22
6
2021
entrez:
22
1
2020
Statut:
ppublish
Résumé
Inducible T-cell costimulator (ICOS) upon binding to its ligand (ICOSL) mediates adaptive immunity and antitumor response. Thus, antitumor therapies targeting the ICOS/ICOSL pathway hold great promise for cancer treatment. In this regard, ICOSL triggering by a soluble recombinant form of ICOS (ICOS-Fc) hampered adhesiveness and migration of dendritic, endothelial, and tumor cells in vitro. Furthermore, in vivo treatment with ICOS-Fc previously showed the capability to inhibit lung metastatization of ICOSL
Identifiants
pubmed: 31962094
pii: S0168-3659(20)30049-3
doi: 10.1016/j.jconrel.2020.01.030
pii:
doi:
Substances chimiques
Icos protein, mouse
0
Inducible T-Cell Co-Stimulator Ligand
0
Inducible T-Cell Co-Stimulator Protein
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
112-124Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest A patent application has been submitted for use of ligands of ICOSL loaded in nanoparticles in tumors treatment.